EP2090555B1 - Radiowellenabsorbierendes material und radiowellenabsorber - Google Patents

Radiowellenabsorbierendes material und radiowellenabsorber Download PDF

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Publication number
EP2090555B1
EP2090555B1 EP07830053.0A EP07830053A EP2090555B1 EP 2090555 B1 EP2090555 B1 EP 2090555B1 EP 07830053 A EP07830053 A EP 07830053A EP 2090555 B1 EP2090555 B1 EP 2090555B1
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Prior art keywords
radio wave
wave absorption
mol
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examples
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English (en)
French (fr)
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EP2090555A1 (de
EP2090555A4 (de
Inventor
Shinroh Itoh
Yasuharu Miyoshi
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Proterial Ltd
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Hitachi Metals Ltd
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Definitions

  • the present invention relates to a radio wave absorption material formed of a sintered ferrite material for absorbing unnecessary radio waves and to a radio wave absorber formed of the radio wave absorption material.
  • radio wave absorbers matching with the respective frequency bands are demanded for the purpose of shutting off high-frequency noise that may cause unnecessary signals.
  • radio wave absorbers those formed of a metal plate, thin film, carbon, etc. having conductivity and being held with rubber, plastic, etc. are generally used.
  • an absorber made of carbonyl iron known as a magnetic absorber, an absorber combined with rubber, etc., and an absorber made of styrofoam, etc. through the use of dielectric loss are also known.
  • absorbers made of composite materials obtained by combining ferrite powders, such as Ni-Zn-based and Ni-Cu-Zn-based ferrite powders, with high molecular compounds, such as rubber, silicone resin and epoxy resin, absorbers made of plastic in which metal foil pieces, such as aluminum foil pieces, are mixed, absorbers made of conductive fiber, etc. have been proposed.
  • Such conventional radio wave absorption materials have inherent matching frequency bands; for example, a radio wave anechoic chamber for use in various experiments and measurements is required not to allow radio waves generated inside the chamber to reflect from the walls thereof and is required to shut off radio waves coming from the outside, and materials excellent in radio wave absorption capability in wide frequency bands are demanded.
  • NiO being expensive among main materials for use in ferrite is used in such Ni-Cu-Zn-based ferrite sintered materials, there occurs a problem that Ni-Cu-Zn-based ferrite tiles produced as radio wave absorbers are high in cost.
  • Mn-Zn-based ferrite sintered materials serving as radio wave absorption materials being equivalent to the Ni-Cu-Zn-based ferrite sintered materials in performance without using such a costly main material as NiO have been proposed (Japanese Patent Application Laid-Open No. 2004-247602 and Japanese Patent Application Laid-Open No. 2004-247603 ).
  • US 2001/0017363 A1 provides a Mn-Zn ferrite having an electrical resistivity exceeding 1 m order and having a high initial permeability of 4000 or more at 100 KHz and 100 or more at 10 MHz.
  • the main components of the Mn-Zn ferrite include 44.0 to 49.8 mol% Fe 2 O 3 , 15.0 to 26.5 mol% ZnO, 0.1 to 3.0 mol% CaO, 0,02 to 1.00 mol% Mn 2 O 3 and the remainder MnO.
  • the obtained sintered core has a component composition including 44.0 to 49.8 mol% Fe 2 O 3 , 4.0 to 26.5 mol% ZnO, 1.0 to 3.0 mol% CaO, 0,02 to 1.00 mol% Mn 2 O 3 and a remainder MnO.
  • radio wave absorbers in which the Mn-Zn-based ferrite sintered materials described in Japanese Patent Application Laid-Open No. 2004-247602 and Japanese Patent Application Laid-Open No. 2004-247603 are used, have insulating phases formed of CaO, etc. in grain boundaries, intergranular failure is apt to occur, and the strength of the ferrite materials is lowered.
  • the strength of the ferrite materials is low, sintered bodies are apt to be broken when they are cut or assembled, whereby not only low yield is caused but also there is a problem that they are difficult to use as radio wave absorbers for use in radio wave anechoic chambers.
  • the change in dielectric constant with respect to humidity is significant due to water absorption in the grain boundary phases formed of CaO.
  • the present invention is intended to provide a radio wave absorption material having high strength and high humidity stability and having performance equivalent to or better than that of the Ni-Cu-Zn-based ferrite sintered materials and to provide a radio wave absorber formed of the radio wave absorption material.
  • a radio wave absorption material according to the present invention is characterized to be obtained by firing a ferrite material that is formed by adding 0.1 to 2 wt% of CoO to an oxide magnetic material containing 30 to 49.5 mol% of Fe 2 O 3 , 0.5 to 20 mol% of Mn 2 O 3 , 5 to 35 mol% of ZnO, 0.2 to 15 mol% of (Li 0.5 Fe 0.5 )O and MnO as the rest.
  • the radio wave absorption material of the present invention is obtained by firing a material formed by adding an accessory component, CoO: 0.1 to 2 wt%, to an oxide magnetic material containing main components, Fe 2 O 3 : 30 to 49.5 mol%, Mn 2 O 3 : 0.5 to 20 mol%, ZnO: 5 to 35 mol%, (Li 0.5 Fe 0.5 )O: 0.2 to 15 mol% and MnO: the rest.
  • the radio wave absorption material of the present invention does not contain NiO, thereby being low in cost. Furthermore, its strength is excellent in comparison with the Mn-Zn-based ferrite sintered material described in Japanese Patent Application Laid-Open No. 2004-247602 or Japanese Patent Application Laid-Open No. 2004-247603 , and change in dielectric constant due to moisture absorption is not seen. Moreover, its radio wave absorption performance is equivalent to or better than that of Ni-Cu-Zn-based ferrite sintered materials.
  • the radio wave absorption material according to the present invention is characterized to contain 20 mol% or less of CuO.
  • part of ZnO is replaced with 20 mol% or less of CuO. Low-temperature sintering is made possible by the replacement with CuO.
  • the radio wave absorption material according to the present invention is characterized to contain at least one of 0.001 to 0.5 wt% of Al 2 O 3 , 0.005 to 1.0 wt% of NiO and 0.005 to 0.4 wt% of Cr 2 O 3 .
  • At least one of Al 2 O 3 : 0.001 to 0.5 wt%, NiO: 0.005 to 1.0 wt% and Cr 2 O 3 : 0.005 to 0.4 wt% is contained as an accessory component, whereby a favorable reflection coefficient of -20 dB or less can be obtained in a wide temperature range of 18 to 30°C.
  • the radio wave absorption material according to the present invention is characterized to contain at least one of 0.002 to 0.095 wt% of a sulfur compound in terms of SO 3 and 0.002 to 0.08 wt% of a chlorine compound in terms of Cl.
  • At least one of a sulfur compound: 0.002 to 0.095 wt% in terms of SO 3 and a chlorine compound: 0.002 to 0.08 wt% in terms of Cl is contained as an accessory component, whereby it is possible to provide a sintered body having small dispersion in the high level of radio wave absorption performance.
  • the radio wave absorption material according to the present invention is characterized to contain at least one of 0.002 to 0.3 wt% of SiO 2 and 0.003 to 0.3 wt% of CaO.
  • the radio wave absorption material of the present invention at least one of SiO 2 : 0.002 to 0.3 wt% and CaO: 0.003 to 0.3 wt% is contained as an accessory component.
  • SiO 2 0.002 to 0.3 wt%
  • CaO 0.003 to 0.3 wt%
  • the radio wave absorption material according to the present invention is characterized in that in the case that the material contains both SiO 2 and CaO, the total amount thereof is 0.5 wt% or less.
  • chipping during cutting can be suppressed from occurring by setting the total amount of SiO 2 and CaO to 0.5 wt% or less.
  • the radio wave absorption material according to the present invention is characterized to contain a 0.001 to 0.08 wt% of a phosphor compound in terms of P 2 O 5 .
  • 0.001 to 0.08 wt% of a phosphor compound in terms of P 2 O 5 is contained as an accessory component, whereby sinterability can be enhanced and stable sintering can be done even in the case that a large compact is sintered.
  • a radio wave absorber according to the present invention is characterized to be formed of the above-mentioned radio wave absorption material.
  • the radio wave absorber of the present invention is produced using the radio wave absorption material having the above-mentioned composition. Hence, a radio wave absorber being low in cost, excellent in reliability and having high radio wave absorption performance is obtained.
  • the radio wave absorber according to the present invention is characterized in that the reflection coefficient thereof for a radio wave of 30 MHz at a thickness of 8 mm or less is -20 dB or less.
  • the reflection coefficient thereof for a radio wave of 30 MHz at a thickness of 8 mm or less is -20 dB or less. Hence, a low reflection coefficient (high absorption performance) is obtained even if the thickness thereof is small.
  • the present invention it is possible to obtain an inexpensive radio wave absorption material having high strength and humidity stability and having radio wave absorption performance equivalent to or better than that of the Ni-Cu-Zn-based ferrite sintered bodies. Hence, a radio wave anechoic chamber having performance equivalent to or better than that of the conventional chambers can be set up at low cost by using the radio wave absorber produced using this radio wave absorption material.
  • a radio wave absorption material according to the present invention is obtained by adjusting components Fe, Mn, Zn and Li serving as main components so as to have ratios in terms of the respective oxides, that is, Fe 2 O 3 : 30 to 49.5 mol%, Mn 2 O 3 : 0.5 to 20 mol%, ZnO: 5 to 35 mol%, (Li 0.5 Fe 0.5 )O: 0.2 to 15 mol% and MnO: the rest, by adding CoO: 0.1 to 2 wt% and by performing firing to form a ferrite compact.
  • Part of ZnO may be replaced with 20 mol% or less of CuO in the composition of the above-mentioned main components.
  • the ratio of trivalent metal oxides is generally made equal to the ratio of divalent metal oxides.
  • the amount of Mn 2 O 3 is determined depending on the amount of Fe 2 O 3 . Since the amount of Fe 2 O 3 is 30 to 49.5 mol% as described above, the amount of Mn 2 O 3 becomes 0.5 to 20 mol% depending thereon.
  • ZnO may be replaced with CuO to perform low-temperature sintering.
  • the replacement is performed such that the amount is more than 20 mol%, no sufficient radio wave absorption performance is obtained, whereby the upper limit of the amount of the replacement is 20 mol%.
  • MnO is contained as the rest corresponding to the respective specified amounts of the above-mentioned Fe 2 O 3 , Mn 2 O 3 , ZnO, (Li 0.5 Fe 0.5 )O and CuO.
  • a favorable reflection coefficient of -20 dB or less in a wide temperature range of 18 to 30°C can be obtained by containing the accessory components having values in the above-mentioned ranges.
  • the contents of any of these accessory components are less than the above-mentioned lower limit values, this effect is not obtained.
  • the crystal grain size of the material becomes minute, and the soft magnetic characteristics thereof are degraded.
  • a sintered body having small dispersion in the high level of radio wave absorption characteristics can be obtained by containing the accessory components having values in the above-mentioned ranges.
  • the contents of any of these accessory components are less than the above-mentioned lower limit values, this effect is not obtained.
  • the crystal grain size of the material becomes minute, and the radio wave absorption characteristics thereof are degraded as ⁇ ' rises.
  • Chipping when the sintered body is cut can be suppressed from occurring by containing the accessory components having values in the above-mentioned ranges.
  • the contents of any of these accessory components are less than the above-mentioned lower limit values, this effect is not obtained.
  • the thickness of the grain boundary phase increases and the crystal grain size becomes minute, whereby the material eventually has a structure in which intergranular failure advances significantly and the strength of the radio wave absorption material lowers.
  • Chipping can be suppressed from occurring by setting the total amount of SiO 2 and CaO to a value in the above-mentioned range.
  • the total amount is more than the above-mentioned upper limit value, the thickness of the grain boundary phase increases and the crystal grain size becomes minute, whereby the material eventually has a structure in which intergranular failure advances significantly and the strength of the radio wave absorption material lowers.
  • the sinterability of the material can be improved by containing a phosphor compound having a value in the above-mentioned range.
  • a phosphor compound having a value in the above-mentioned range In the case that the content of the phosphor compound is less than the above-mentioned lower limit value, this effect is not obtained.
  • the content of the phosphor compound is more than the above-mentioned upper limit value, the growth of crystal grain size is non-uniform and advances excessively, that is, exaggerated grain growth occurs, whereby the soft magnetic characteristics are degraded and the mechanical strength lowers.
  • radio wave absorption materials in which the composition ratios of various metal oxides were changed, were produced, and the performance values (reflection coefficients) of radio wave absorbers formed of the produced radio wave absorption materials were measured; the results of the measurement are described.
  • the production conditions and performance (reflection coefficient) measurement conditions for the radio wave absorption materials in these Examples and Comparison examples are determined as described below.
  • Raw powders were mixed so that composition ratios described later were obtained finally, and the powders were calcinated temporarily fired in atmospheric air at 850°C for 3 hours.
  • the obtained calcinated powders were wet-milled using a ball mill and then dried.
  • 7 wt% solution of polyvinyl alcohol was added at 14 wt%, and a granular powder was obtained.
  • the granular powder was molded into a compact having a disc shape measuring 62 mm in diameter x 10 mm in thickness at 1.5 ton/cm 2 .
  • the obtained compact was heated to 1300°C at a rate of 150°C/hour or less in the atmospheric air, and the temperature was kept for 3 hours.
  • the atmosphere was changed to a nitrogen atmosphere, and the temperature was lowered to room temperature at a rate of 200°C/hour or less.
  • a ring-shaped test piece measuring approximately 39 mm in outside diameter x approximately 17 mm in inside diameter x 6.7 mm in thickness was cut out from the obtained disc-shaped sintered body, and the impedance of the test piece was measured using a network analyzer.
  • the impedance-matching thickness is 6.7 mm or more
  • a test piece with thickness of 6.7 mm is used and the reflection coefficient for a radio wave of 30 MHz was measured by the network analyzer.
  • the impedance-matching thickness is less than 6.7 mm, a test piece was further subjected to grinding so as to have a thickness equal to the impedance-matching thickness and then the reflection coefficient was measured.
  • FIG. 1 is a table showing the compositions of the respective metal oxides and the measured reflection coefficients for a radio wave of 30 MHz in the radio wave absorption materials of Examples 1 to 7 and Comparison examples 1 and 2. In the combinations in these Examples 1 to 7 and Comparison examples 1 and 2, the composition ratio of Fe 2 O 3 is made different.
  • FIG. 2 is a table showing the compositions of the respective metal oxides and the measured reflection coefficients for a radio wave of 30 MHz in the radio wave absorption materials of Examples 8 to 11 and Comparison examples 3 and 4. In the combinations in these Examples 8 to 11 and Comparison examples 3 and 4, the composition ratio of ZnO is made different.
  • FIG. 3 is a table showing the compositions of the respective metal oxides and the measured reflection coefficients for a radio wave of 30 MHz in the radio wave absorption materials of Examples 12 to 14 and Comparison examples 5 and 6.
  • the composition ratio of (Li 0.5 Fe 0.5 )O is made different.
  • FIG. 4 is a table showing the compositions of the respective metal oxides in the radio wave absorption materials of Experiment examples A, B and C.
  • FIG. 5 is a graph showing the relationship between the wt% of CoO and the measured reflection coefficient for a radio wave of 30 MHz in the case that the wt% of CoO was changed in Experiment examples A, B and C.
  • the reflection coefficients of all the radio wave absorption materials in Examples 1 to 14 in which the conditions of the composition ratios of the present invention are satisfied are -20dB or less as described above, and it is found that ferrite sintered bodies having excellent radio wave absorption performance are obtained according to the present invention. Furthermore, although the reflection coefficients for a radio wave of 30 MHz have been described, excellent radio wave absorption performance values (reflection coefficients of -20 dB or less) are obtained for a radio wave having a frequency band of 30 to several hundred MHz required for radio wave anechoic chambers.
  • ⁇ ' (the real part of complex relative magnetic permeability) is 50 or less and ⁇ " (the imaginary part of complex relative magnetic permeability) is 200 or more in all the radio wave absorption materials in Examples 1 to 14 described above, whereby the materials have characteristics so as to serve as excellent radio wave absorption materials.
  • radio wave absorption materials in which the content wt% values of accessory components were changed were produced, and the characteristics of various radio wave absorbers formed of the produced radio wave absorption materials were measured; the results of the measurement are described.
  • the production conditions and reflection coefficient measurement conditions for the radio wave absorption materials in these Examples and Comparison examples are similar to those described above.
  • FIG. 6 is a table showing the compositions, the reflection coefficients for a radio wave of 30 MHz at 18 to 30°C and the average grain size of the radio wave absorption materials of Examples 15 to 29 and Comparison examples 7 to 15.
  • the content (wt%) of at least one of Al 2 O 3 , NiO and Cr 2 O 3 is made different.
  • FIG. 7 is a table showing the compositions, the reflection coefficients for a radio wave of 30 MHz, the dispersion in radio wave absorption performance and the average grain size of the radio wave absorption materials of Examples 30 to 37 and Comparison examples 16 to 21.
  • the content of at least one of the sulfur compound and the chlorine compound (wt% in terms of SO 3 , wt% in terms of Cl) is made different.
  • the dispersion in the radio wave absorption performance was measured as described below. On the basis of the difference between the highest and lowest reflection coefficient values in each of 30 sintered bodies sintered at the same time, the magnitude of the dispersion in the radio wave absorption performance among the sintered bodies was evaluated. More specifically, in the case that the difference between the highest and lowest reflection coefficient values was 2 dB or less, the dispersion in the radio wave absorption performance was evaluated small ( ⁇ in FIG. 7 ), and in the case that the difference was more than 2 dB, the dispersion in the radio wave absorption performance was evaluated large ( ⁇ in FIG. 7 ).
  • FIG. 8 is a table showing the compositions, the reflection coefficients for a radio wave of 30 MHz, the transverse strength and the degree of chipping in the radio wave absorption materials of Examples 38 to 46 and Comparison examples 22 to 29.
  • the content (wt%) of at least one of SiO 2 and CaO is made different.
  • the transverse strength values are obtained as the measurement results of the three-point bending test conforming to JIS-R1601. Furthermore, with respect to the degree of chipping, in the case that the size of the chipping occurred at the end portion of the test piece was less than 5 mm when the test piece was processed in the direction of the thickness thereof using a double-side grinding machine equipped with #120 grinding stones, the chipping was evaluated small ( ⁇ in FIG. 8 ), and in the case that the size was 5 mm or more, the chipping was evaluated large (x in FIG. 8 ).
  • FIG. 9 is a table showing the compositions, the reflection coefficients for a radio wave of 30 MHz, the relative density of the sintered body, the interstage dispersion in characteristics and the transverse strength in the radio wave absorption materials of Examples 47 to 50 and Comparison examples 30 to 32.
  • the content of the phosphor compound (wt% in terms of P 2 O 5 ) is made different.
  • the sinterability can be evaluated by comparing the relative density values of the obtained sintered bodies. More specifically, in the case that the relative density values are 98% or more, the sinterability can be evaluated good, and in the case that the relative density values are less than 98%, the sinterability can be evaluated bad.
  • the interstage dispersion in characteristics was evaluated according to the method described below.
  • a five-stage sintering shelf was formed in a furnace by combining plates measuring 150 mm x 150 mm x 5 mm in thickness and spacers measuring 15 mm ⁇ 15 mm ⁇ 15 mm, both being made of refractory materials, each one of compacts obtained by performing molding into a disc shape measuring 62 mm in diameter ⁇ 10 mm in thickness at 1.5 ton/cm 2 was placed on each stage, and the compact was fired under the above-mentioned conditions. Then, ring-shaped test pieces were cut out in a way similar to that described above, and the impedance values thereof were measured.
  • the reflection coefficients for a radio wave of 30 MHz were measured under the above-mentioned measurement conditions and the dispersion values in the reflection coefficients of the sintered bodies obtained in the respective stages were compared and evaluated.
  • the measured value at 6.7 mm was used for comparison; in the case of a test piece having a matching thickness of less than 6.7 mm, it was subjected to grinding so as to have a matching thickness, and the measured value at the thickness was used for comparison.
  • the dispersion in the measured values was evaluated; that is, in the case that the difference was less than 2 dB, the dispersion was evaluated small, and in the case that the difference was 2 dB or more, the dispersion was evaluated large.
  • the transverse strength values are obtained as the measurement results of the three-point bending test conforming to JIS-R1601, just as in the above-mentioned examples.
  • a radio wave absorption material comprising main components, Fe 2 O 3 : 41.5 mol%, Mn 2 O 3 : 8.5 mol%, MnO: 24.1 mol%, ZnO: 19.7 mol%, (Li 0.5 Fe 0.5 )O: 2.7 mol% and CuO: 3.5 mol% and further containing accessory components, CoO: 0.67 wt%, Cr 2 O 3 : 0.028 wt%, a sulfur compound: 0.065 wt% in terms of SO 3 , SiO 2 : 0.013 wt% and a phosphor compound: 0.026 wt% in terms of P 2 O 5 , has a favorable reflection coefficient of -20 dB or less in a wide temperature range of 18 to 30°C, is satisfactory in sinterability, and is free from the problems of dispersion in performance and the occurrence of chipping during cutting, whereby both excellent radio wave absorption performance and excellent production stability can be attained.
  • a radio wave absorption material containing all of Al 2 O 3 , NiO, Cr 2 O 3 , a sulfur compound, a chlorine compound, SiO 2 , CaO and a phosphor compound, having values in the above-mentioned predetermined ranges, as accessory components can attain all of the following: a favorable reflection coefficient of -20 dB or less in a wide temperature range of 18 to 30°C, small dispersion in the high level of radio wave absorption characteristics, suppression of chipping occurrence and stable sintering of large compacts.
  • a radio wave absorption material comprising main components, Fe 2 O 3 : 45.2 mol%, Mn 2 O 3 : 4.8 mol%, MnO: 29.8 mol%, ZnO: 19.1 mol% and (Li 0.5 Fe 0.5 )O: 1.1 mol%, further containing accessory components, CoO: 0.55 wt%, Al 2 O 3 : 0.006 wt%, NiO: 0.012 wt% and Cr 2 O 3 : 0.013 wt%, and having an average grain size of 13 ⁇ m was produced, and the reflection coefficient for a radio wave of 30 MHz in a radio wave absorber formed of the produced radio wave absorption material was measured in a temperature range of 10 to 40°C. The measurement results are shown in FIG. 10 .
  • This example has a favorable reflection coefficient of -20 dB or less in the wide temperature range of 10 to 40°C.

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Claims (9)

  1. Radiowellenabsorptionsmaterial, dadurch gekennzeichnet, dass es durch Brennen eines Ferritmaterials erhältlich ist, welches durch Hinzufügen von 0,1 bis 2 Gew.-% CoO zu einem magnetischen Oxidmaterial, das 30 bis 49,5 Mol-% Fe2O3, 0,5 bis 20 Mol-% Mn2O3, 5 bis 35 Mol-% ZnO, 0,2 bis 15 Mol-% (Li0,5Fe0,5)O und MnO als Rest enthält, gebildet wird.
  2. Radiowellenabsorptionsmaterial gemäß Anspruch 1, wobei das magnetische Oxidmaterial 20 Mol-% oder weniger CuO enthält.
  3. Radiowellenabsorptionsmaterial gemäß Anspruch 1, das wenigstens eines aus 0,001 bis 0,5 Gew.-% Al2O3, 0,005 bis 1,0 Gew.-% NiO und 0,005 bis 0,4 Gew.-% Cr2O3 enthält.
  4. Radiowellenabsorptionsmaterial gemäß Anspruch 1, das wenigstens eines aus 0,002 bis 0,095 Gew.-% einer Schwefelverbindung als SO3 und 0,002 bis 0,08 Gew.-% einer Chlorverbindung als Cl enthält.
  5. Radiowellenabsorptionsmaterial gemäß Anspruch 1, das wenigstens eines aus 0,002 bis 0,3 Gew.-% SiO2 und 0,003 bis 0,3 Gew.-% CaO enthält.
  6. Radiowellenabsorptionsmaterial gemäß Anspruch 5, wobei in dem Fall, dass das Material sowohl SiO2 als auch CaO enthält, die Gesamtmenge davon 0,5 Gew.-% oder weniger beträgt.
  7. Radiowellenabsorptionsmaterial gemäß Anspruch 1, das 0,001 bis 0,08 Gew.-% einer Phosphorverbindung als P2O5 enthält.
  8. Radiowellenabsorber, der aus dem Radiowellenabsorptionsmaterial gemäß einem der Ansprüche 1 bis 7 gebildet ist.
  9. Radiowellenabsorber gemäß Anspruch 8, wobei sein Reflexionskoeffizient für eine Radiowelle von 30 MHz bei einer Dicke von 8 mm oder weniger -20 dB oder weniger beträgt.
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CN101511751A (zh) 2009-08-19
JPWO2008047854A1 (ja) 2010-02-25
US8138959B2 (en) 2012-03-20
EP2090555A1 (de) 2009-08-19
CN101511751B (zh) 2012-11-21
EP2090555A4 (de) 2011-04-27
WO2008047854A1 (en) 2008-04-24
KR101121554B1 (ko) 2012-03-06
JP4935824B2 (ja) 2012-05-23
KR20090074079A (ko) 2009-07-03
US20100045505A1 (en) 2010-02-25

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